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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>19</Volume><Issue>4</Issue></Journal><ArticleTitle>Gastroprotective activity of α-terpineol in two experimental models of gastric ulcer in rats.</ArticleTitle><FirstPage>277</FirstPage><LastPage>81</LastPage><AuthorList><Author><FirstName>Rhl</FirstName><LastName>Souza</LastName></Author><Author><FirstName>Msp</FirstName><LastName>Cardoso</LastName></Author><Author><FirstName>Ct</FirstName><LastName>Menezes</LastName></Author><Author><FirstName>Jp</FirstName><LastName>Silva</LastName></Author><Author><FirstName>Dp</FirstName><LastName>De Sousa</LastName></Author><Author><FirstName>Js</FirstName><LastName>Batista</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>11</Month><Day>09</Day></PubDate></History><Abstract>Several plant essential oils, as well as terpenes present in essential oils, have shown gastroprotective activity. The aim of the present work was to evaluate the gastroprotective activity of α-terpineol, a monoterpene alcohol which is present in essential oils of various plants.The gastroprotective activity of α-terpineol was evaluated in rats by assessing the changes in ethanol and indomethacin-induced gastric ulcer scores and on gastric secretory volume and total acidity in pylorus-ligated rats. Alpha-terpineol was administrated orally at the doses of 10, 30, and 50 mg/kg one hour before administration of the ulcer inducing agents by the pylorus ligation procedure. The involvement of endogenous prostaglandins in the protective effect of α-terpineol in ethanol-induced gastric lesions test was assessed by administration of indomethacin (10 mg/kg, s.c.) 30 min before oral administration of α-terpineol at the dose of 50 mg/kg.α-terpineol presented gastroprotective activity against ethanol-induced ulcers at the doses of 10, 30, and 50 mg/kg. Epoxy-carvone at the dose of 10 mg/kg did not present gastroprotective activity against ulcer induced by indomethacin, but at the doses of 30 and 50 mg/kg it attenuated the gastric damages induced by this agent significantly. Pretreatment with indomethacin did not prevent the gastroprotective effect of α-terpineol on ethanol-induced ulcers. Alpha-terpineol also did not affect the gastric secretion in pylorus-ligated rats.The results suggest that α-terpineol presents gastroprotective action which does not involve either an increase in the synthesis of endogenous prostaglandin or a decrease in the gastric acid secretion.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/415</web_url></Article></Articles>
